| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:66366467-66366483 | Rare:2 | ||||
| chr16:66366495-66366753 | Common:3; Rare:54 | ||||
| chr16:66552520-66552684 | Rare:67 | ||||
| chr16:66605163-66605274 | Common:1; Rare:23 | ||||
| chr16:66605387-66605538 | Common:2; Rare:46 | ||||
| chr16:66934347-66934711 | Common:1; Rare:104 | ||||
| chr16:67109804-67109994 | Rare:61 | ||||
| chr16:67183559-67183770 | Rare:55 | ||||
| chr16:67183941-67184140 | Common:1; Rare:58 | ||||
| chr16:67227008-67227163 | Rare:62 | ||||
| chr16:67247440-67247767 | Common:1; Rare:97 | ||||
| chr16:67481057-67481384 | Common:1; Rare:118 | ||||
| chr16:67528728-67528883 | Rare:41 | ||||
| chr16:67660227-67660364 | Rare:80; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:67719241-67719473 | Common:1; Rare:63 |